Thermo Scientific Chemicals

Mercaptoacetic acid, 97+%, Thermo Scientific Chemicals

Catalog number: B20391.0E
2500 g, Each
Thermo Scientific Chemicals

Mercaptoacetic acid, 97+%, Thermo Scientific Chemicals

Catalog number: B20391.0E
2500 g, Each
Quantity
Catalog number: B20391.0E
also known as B20391-0E
Price (EUR)
Quantity
-

Chemical Identifiers

CAS
68-11-1
IUPAC Name
2-sulfanylacetic acid
Molecular Formula
C2H4O2S
InChI Key
CWERGRDVMFNCDR-UHFFFAOYSA-N
SMILES
OC(=O)CS
Comment
Material sourced in the U.S. and in other countries
Identification (FTIR)
Conforms (non-U.S. sourced material)
Proton NMR
Conforms to structure (non-U.S. sourced material)
Refractive Index
1.5020-1.5070 @ 20°C (non-U.S. sourced material)
Form
Liquid

Description

Reagent that protects tryptophan in amino acid analysis.Mercaptoacetic acid is used as a protecting agent for tryptophan in amino acid analysis and an acidity indicator. It finds application as an intermediate in the chemical reactions such as addition, elimination and cyclization. It acts as a precursor to ammonium thioglycolate, sodium thioglycolate and calcium thioglycolate. Its organotin derivatives are used as stabilizers for polyvinyl chloride (PVC). In organic synthesis, it acts as a nucleophile in thioglycolysis reactions and sulfur transfer agent for sulfonyl chloride synthesis. Further, it is used in leather processing.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Reagent that protects tryptophan in amino acid analysis.Mercaptoacetic acid is used as a protecting agent for tryptophan in amino acid analysis and an acidity indicator. It finds application as an intermediate in the chemical reactions such as addition, elimination and cyclization. It acts as a precursor to ammonium thioglycolate, sodium thioglycolate and calcium thioglycolate. Its organotin derivatives are used as stabilizers for polyvinyl chloride (PVC). In organic synthesis, it acts as a nucleophile in thioglycolysis reactions and sulfur transfer agent for sulfonyl chloride synthesis. Further, it is used in leather processing.

Solubility
Miscible with water, ethanol, ethers, ketones, esters, chlorinated hydrocarbons, benzene and aromatic hydrocarbons. Slightly miscible with chloroform.

Notes
Air sensitive. Incompatible with strong oxidizing agents and strong acids.
RUO – Research Use Only

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    Safety and Handling


    Classification of the substance or mixture
    CLP classification - Regulation(EC) No 1272/2008
    Acute oral toxicity
    Category 3
    Acute dermal toxicity
    Category 3
    Acute Inhalation Toxicity - Vapors
    Category 4
    Skin Corrosion/Irritation
    Category 1
    Serious Eye Damage/Eye Irritation
    Category 1
    Skin Sensitization
    Category 1
    Label Elements
    Signal Word

    Danger

    Hazard Statements

    H301 + H311 - Toxic if swallowed or in contact with skin

    H314 - Causes severe skin burns and eye damage

    H317 - May cause an allergic skin reaction

    H332 - Harmful if inhaled

    Precautionary Statements

    P280 - Wear protective gloves/protective clothing/eye protection/face protection

    P301 + P330 + P331 - IF SWALLOWED: Rinse mouth. Do NOT induce vomiting

    P303 + P361 + P353 - IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse skin with water or shower

    P304 + P340 - IF INHALED: Remove person to fresh air and keep comfortable for breathing

    P305 + P351 + P338 - IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing

    P310 - Immediately call a POISON CENTER or doctor/physician